A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14388708



Internal ID22243806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11789828..11790079hg38UCSC Ensembl
chr16:11883684..11883935hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229988
Supporting Variants
SamplesHG00733
Known GenesZC3H7A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14388708
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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